510(k) Report

FDA applicant

Aesthetic Lasers, Inc.

Annapolis, MD1 decision1996–19960 recalls

FDA records 1 decision for Aesthetic Lasers, Inc. (Annapolis, MD) in 1996: 1 510(k) clearance. All are in product code GFE (Brush, Dermabrasion, Powered). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Aesthetic Lasers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aesthetic Lasers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Aesthetic Lasers, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Aesthetic Lasers, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GFEBrush, Dermabrasion, Powered1decision

What has FDA decided for it lately?

  • K963204DMS-1000C DermoabraderAesthetic Lasers, Inc. · 1996

The one decision as Aesthetic Lasers, Inc. →

Other applicant names beginning “Aesthetic”

FDA records each applicant name separately; these may or may not be the same firm.

Aesthetic and Reconstructive Technologies, Inc. 10Aesthetic Technology, Ltd. 4Aesthetic Management Partners 1Aesthetic-Press, LLC 1